137938609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34574262-A-G

137939058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34574678-G-T

http://identifiers.org/hco/5/GRCh38#137939115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34574733-C-A

137939157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34574765-A-T

137939431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34574980-T-G

http://identifiers.org/hco/5/GRCh38#137939452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34574999-C-A

137939452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34574999-C-T

137939517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575048-T-C

137939517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575048-T-G

137939570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575097-G-A

137939570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575097-G-T

137939587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575114-C-T

137939601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575128-A-G

137939601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575128-A-T

137939676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575198-T-C

137939733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575249-T-C

137939745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575259-G-A

137939745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575259-G-C

137939745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575259-G-T

http://identifiers.org/hco/5/GRCh38#137939781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34575294-C-A

137939781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34575294-C-T

137940496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34575933-T-A

137941854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576863-T-C

137942861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578316-A-T

137942950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34578405-G-C

137943208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34578660-T-C

137943239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578688-T-A

137943239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578688-T-C

137943296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578744-G-A

137943296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578744-G-C

137943296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578744-G-T

137943301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578749-T-C

137943301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578749-T-G

http://identifiers.org/hco/5/GRCh38#137946101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34581298-C-A

137946101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34581298-C-T

137946104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34581301-A-T

137946121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34581318-T-C

http://identifiers.org/hco/5/GRCh38#137946142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34581341-C-A

137946142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34581341-C-T

http://identifiers.org/hco/5/GRCh38#137946267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34581460-C-A

137946267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34581460-C-T

137946318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34581511-T-A

http://identifiers.org/hco/5/GRCh38#137946412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34581558-A-C

137946412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34581558-A-G

137946412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34581558-A-T

http://identifiers.org/hco/5/GRCh38#137946431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34581576-C-A

137946431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34581576-C-T

137948042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583129-C-T

137948105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583177-T-C

137948133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583205-A-G

137948818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584134-A-G

137952721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34587180-T-C

137953119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34587513-G-A

http://identifiers.org/hco/5/GRCh38#137953251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34587636-C-A

137953298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34587669-T-A

137954120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34590674-G-T

137954189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34590740-T-C

137954189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34590740-T-G

137954219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 34590770-G-A

137954288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34590839-G-C

137954288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34590839-G-T

137954295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34590846-T-C

137954424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34590974-G-A

137954424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34590974-G-C

137954424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34590974-G-T

137954950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34591104-T-C

137955489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34591650-C-T

137955925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592064-C-G

137956059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592067-T-C

137956229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592185-C-T

137956384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592321-G-A

137956384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592321-G-T

137956385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592322-A-G

137956385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592322-A-T

http://identifiers.org/hco/5/GRCh38#137956468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34592401-C-A

137956468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592401-C-T

137956539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34592472-G-A

137956539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 34592472-G-T

137956622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592556-A-G

137956623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592557-G-A

137956623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592557-G-T

137956692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34592625-T-A

137957104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34593112-T-C

137958081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34593679-C-T

137958409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34593926-T-C

137958412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34593929-C-G

137959171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34594565-T-C

137959184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34594578-G-A

137959202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34594598-T-G

137959722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34595220-T-C

http://identifiers.org/hco/5/GRCh38#137959879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34595395-C-A

137960042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34595827-A-G

137960110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34595956-T-A

137960110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34595956-T-C

137960110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34595956-T-G

137960163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34596011-T-C

137960178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34596026-T-C

137960308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34596160-G-C

137960308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34596160-G-T

http://identifiers.org/hco/5/GRCh38#137960368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34596221-C-A

137960368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34596221-C-G

137960368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34596221-C-T

137960436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34596288-G-C

137960483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34596340-C-T

137960506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34596363-C-T

137961278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34597221-C-T

137961956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34597777-C-T

137962221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34598020-G-A

http://identifiers.org/hco/5/GRCh38#137962255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34598051-C-A

137962255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34598051-C-T

137962275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34598073-C-G

137962278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34598076-G-A

137962278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34598076-G-T

137962291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34598090-G-A

137962291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34598090-G-C

137962291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34598090-G-T

137985070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34606441-A-G

137985070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34606441-A-T

137985125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34606500-T-C

137985147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34606522-T-A

137985147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34606522-T-C

http://identifiers.org/hco/5/GRCh38#137985213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34606572-C-A

137985213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34606572-C-T

137985373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34606722-C-T

137985487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607257-A-G

http://identifiers.org/hco/5/GRCh38#137985488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34607258-C-A

137985488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607258-C-T

137986029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607702-C-T

137986527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34608373-T-C

137986527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34608373-T-G

137986543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34608389-G-A

137986543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34608389-G-T

http://identifiers.org/hco/5/GRCh38#137987686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34609735-C-A

137987686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609735-C-T

137987792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609838-T-C

http://identifiers.org/hco/5/GRCh38#138006692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34619567-C-A

138006794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34619671-T-C

138006866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34619733-T-C

138006985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34620026-A-G

138007153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34620198-T-C

138010872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34627107-A-T

138010875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34627110-T-C

http://identifiers.org/hco/5/GRCh38#138010916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34627151-C-A

138010916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34627151-C-T

http://identifiers.org/hco/5/GRCh38#138011976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34627859-A-C

138011976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34627859-A-G

138011976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34627859-A-T

138012138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34628021-G-A

138012262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34628125-C-T

138012298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34628161-A-G

138012547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34628464-T-A

138012609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34628586-T-C

http://identifiers.org/hco/5/GRCh38#138012640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34628617-C-A

138012698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34628671-G-T

http://identifiers.org/hco/5/GRCh38#138019247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34631335-A-C

138019247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34631335-A-G

138019293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34631383-A-G

138019303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34631393-G-A

138019889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34631884-C-G

138019889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34631884-C-T

138021132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34632840-C-T

138021176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34632884-G-A

138021176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34632884-G-T

138021224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34632935-T-C

138028341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34634661-T-C

138028483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34634787-G-A

138028483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34634787-G-C

138028483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34634787-G-T

138028486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34634790-T-A

138028486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34634790-T-C

138028690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34634981-C-G

138029219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34635461-G-T

138031312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34638486-G-A

138032204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639000-G-C

138032217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639012-G-C

138032396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34639219-G-A

138032606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34639386-G-C

http://identifiers.org/hco/5/GRCh38#138032631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34639411-C-A

138032631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34639411-C-T

138032662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34639449-A-G

138032704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34639492-G-A

138032705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34639493-G-A

138032726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639527-C-T

138032755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34639555-G-T

138032792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34639592-G-A

138032898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34639698-T-C

138032898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34639698-T-G

138032998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639795-G-A

138032998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639795-G-T

http://identifiers.org/hco/5/GRCh38#138033029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34639838-C-A

138033029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639838-C-T

138033067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639876-G-A

138033067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639876-G-C

138033067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639876-G-T

http://identifiers.org/hco/5/GRCh38#138033075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#34639885-C-A

138033075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34639885-C-T

138033094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34639905-G-A

138033094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34639905-G-T

138033118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34639922-G-T

http://identifiers.org/hco/5/GRCh38#138033178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34639947-C-A

138033178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639947-C-G

http://identifiers.org/hco/5/GRCh38#138033179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34639948-C-A

138033179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639948-C-G

138033179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639948-C-T

138033204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639967-G-A

138033204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639967-G-T

138033207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639970-T-A

138033207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639970-T-C

138033223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639986-T-A

138033223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34639986-T-C

138033256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34640007-G-A

138033286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34640031-G-A

138033356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34640102-C-G

138033630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34640354-A-G

138033646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34640370-G-A

138033646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34640370-G-T

138033653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34640377-G-C

138033653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34640377-G-T

http://identifiers.org/hco/5/GRCh38#138033674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34640398-C-A

138033674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34640398-C-T

138033909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34640733-T-A

138033909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34640733-T-C

138033967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34640797-A-G

138034084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34641268-A-G

138034787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34643705-T-C

138035763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34644722-A-G

138036088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34645007-G-A

138036088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34645007-G-T

138036325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34645162-T-C

138036355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34645191-A-G

138036381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34645210-G-T

138036440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34645269-C-T

138036541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34645359-G-A

138036729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34645536-G-A

138037126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34646349-T-C

138037267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34646464-T-C

138037674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34646840-G-A

138037674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34646840-G-T

138037702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34646867-T-C

138037748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34646902-G-A

http://identifiers.org/hco/5/GRCh38#138038733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34648719-C-A

138038733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34648719-C-T

138039379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34649321-C-T

http://identifiers.org/hco/5/GRCh38#138039434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34649369-C-A

138039434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34649369-C-T

138051192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron variant
orthologous variants: 34654762-C-G

138051306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron variant
orthologous variants: 34654865-T-A

http://identifiers.org/hco/5/GRCh38#138051526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#34655643-A-C

138051778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: intron variant
orthologous variants: 34655919-G-T

138051900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5 prime UTR variant
orthologous variants: 34656025-G-T

138052155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1335
most severe consequence: 5 prime UTR variant
orthologous variants: 34656287-C-T